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Pain and immunity: implications for host defence

Journal

NATURE REVIEWS IMMUNOLOGY
Volume 19, Issue 7, Pages 433-447

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/s41577-019-0147-2

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Funding

  1. US National Institutes of Health (NIH) [NCCIH DP2AT009499, RO1AI130019]
  2. Chan-Zuckerberg Initiative
  3. Harvard Stem Cell Institute
  4. NIH [T32 AI007061]

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Pain is a hallmark of tissue injury, inflammatory diseases, pathogen invasion and neuropathy. It is mediated by nociceptor sensory neurons that innervate the skin, joints, bones, muscles and mucosal tissues and protects organisms from noxious stimuli. Nociceptors are sensitized by inflammatory mediators produced by the immune system, including cytokines, lipid mediators and growth factors, and can also directly detect pathogens and their secreted products to produce pain during infection. Upon activation, nociceptors release neuropeptides from their terminals that potently shape the function of innate and adaptive immune cells. For some pathogens, neuron-immune interactions enhance host protection from infection, but for other pathogens, neuron-immune signalling pathways can be exploited to facilitate pathogen survival. Here, we discuss the role of nociceptor interactions with the immune system in pain and infection and how understanding these pathways could produce new approaches to treat infectious diseases and chronic pain.

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